Total: 18 |
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PMID (PMCID) | ||
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30636638 |
FEMALE | Middle Aged |
The additional genetic diagnosis of homozygous sickle cell disease in a patient with Waardenburg-Shah syndrome: a case report. | ||
Rankine-Mullings AE, Serjeant G, Ramsay Z, Hanchard NA, Asnani M. J Med Case Rep. 2019;13(1):10. |
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The complications of sickle cell disease she experienced included bone pain, a chronic right leg ulcer, avascular necrosis of her left hip, and symptomatic cholelithiasis. | ||
25053687 |
FEMALE | Adult |
Adrenal myelolipoma, cholelithiasis and calcified spleen: retrospective diagnosis of sickle cell anemia using a novel triad of abdominal imaging findings. | ||
Jakhere SG, Kumbhar RS, Dhongade HV. Acta Med Indones. 2014;46(2):134-7. |
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Adrenal myelolipoma, cholelithiasis and calcified spleen: retrospective diagnosis of sickle cell anemia using a novel triad of abdominal imaging findings. | ||
27366449 |
OTHER | |
Perioperative Anaesthetic Approach in a Homozygous Sickle Cell Anaemia Patient with Frequent Pain Crises. | ||
Tuzcu K, Karcoglu M, Davarc I, Hakimoglu S, Akkucuk S. Turk J Anaesthesiol Reanim. 2014;42(6):348-51. |
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In patients with sickle cell disease, high rates of erythrocyte generation, degradation, and hyperbilirubinemia increase the risk for cholelithiasis. | ||
21655030 (3101768) |
OTHER | |
Anesthetic management of a patient with sickle beta thalassemia. | ||
Bharati S, Das S, Majee P, Mandal S. Saudi J Anaesth. 2011;5(1):98-100. |
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We are reporting a 14-year-old girl diagnosed with sickle cell anemia and 946(+) thalassemia with cholelithiasis went for cholecystectomy under general anesthesia. | ||
21642788 |
MALE | |
Cholelithiasis in a toddler with sickle cell disease. | ||
Schinasi DA, Mistry RD, Mistry R. Pediatr Emerg Care. 2011;27(6):533-4. |
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Cholelithiasis is rarely seen in toddlers and school-aged children, even in the setting of sickle cell anemia. | ||
21642788 |
MALE | |
Cholelithiasis in a toddler with sickle cell disease. | ||
Schinasi DA, Mistry RD, Mistry R. Pediatr Emerg Care. 2011;27(6):533-4. |
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We describe a case of a toddler with sickle cell disease initially presenting with abdominal pain who was found to have symptomatic cholelithiasis. | ||
12817741 |
FEMALE | Child |
Treatment of cholelithiasis in children with sickle cell disease. | ||
Hendricks-Ferguson V, Nelson MA. AORN J. 2003;77(6):1170-8, 1181-2; quiz 1185-8. |
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Treatment of cholelithiasis in children with sickle cell disease. | ||
19658360 |
MALE | |
[Laparoscopic cholecystectomy in a child with sickle cell disease]. | ||
Antabak A, Skegro M, Batinica S, Zupancic B, Popovic L. Lijec Vjesn. 1998;120(12):376-8. |
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Laparoscopic cholecystectomy is the procedure of choice in the management of cholelithiasis in small children and infants, especially those with sickle cell disease. | ||
19658360 |
MALE | |
[Laparoscopic cholecystectomy in a child with sickle cell disease]. | ||
Antabak A, Skegro M, Batinica S, Zupancic B, Popovic L. Lijec Vjesn. 1998;120(12):376-8. |
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One of them was a five year old boy with sickle cell disease and cholelithiasis. | ||
19658360 |
MALE | |
[Laparoscopic cholecystectomy in a child with sickle cell disease]. | ||
Antabak A, Skegro M, Batinica S, Zupancic B, Popovic L. Lijec Vjesn. 1998;120(12):376-8. |
||
Before the advent of laparoscopy, few children with sickle cell disease and cholelithiasis underwent cholecystectomy, because of the high morbidity associated with open cholecystectomy. | ||
9659743 |
MALE | Adult |
[Laparoscopic cholecystectomy in a patient with sickle-cell anemia]. | ||
Machado MA, Rocha JR, Bove C, Jukemura J, Montagnini AL, Penteado S, Machado MC. Rev Hosp Clin Fac Med Sao Paulo. 1998;53(1):39-41. |
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Elective surgical treatment of cholelithiasis in patients with sickle cell anemia has been followed by frequent postoperative complications. | ||
3344739 |
FEMALE | Adult |
Hepatic portal venous gas due to endoscopic sphincterotomy. | ||
Simmons TC. Am J Gastroenterol. 1988;83(3):326-8. |
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This report describes a patient with sickle cell disease and cholelithiasis with choledocholithiasis who developed benign hepatic portal venous gas following endoscopic sphincterotomy. | ||
6698374 |
FEMALE | Adult |
Hepatic biloma complicating sickle cell disease. A case report and a review of the literature. | ||
Middleton JP, Wolper JC. Gastroenterology. 1984;86(4):743-4. |
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Previously reported hepatobiliary complications of sickle cell disease include cholelithiasis, intrahepatic cholestasis, cirrhosis, hepatic crisis, abscess, and infarction. | ||
7205988 |
FEMALE | Adult |
Cholelithiasis: a differential diagnosis in abdominal "crisis" of sickle cell anemia. | ||
Matthews MS. J Natl Med Assoc. 1981;73(3):271-3. |
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Cholelithiasis: a differential diagnosis in abdominal "crisis" of sickle cell anemia. | ||
453236 |
MIXED_SAMPLE | Child |
Cholelithiasis in sickle cell anemia: a case for elective cholecystectomy. | ||
Solanki DL, McCurdy PR. Am J Med Sci. 1979;277(3):319-24. |
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Cholelithiasis in sickle cell anemia: a case for elective cholecystectomy. | ||
951141 |
MALE | |
Cholecystitis and cholelithiasis masking as abdominal crises in sickle cell disease. | ||
Ariyan S, Shessel FS, Pickett LK. Pediatrics. 1976;58(2):252-8. |
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Some physicians and pediatricians believe that (1) cholelithiasis and cholecystitis are uncommon in sickle cell disease; (2) the complications of gallstones are not significant; (3) the operative risk in patients with sickle cell disease is high; (4) these patients with HbSS disease do not live long enough to get into trouble with gallstones. | ||
951141 |
MALE | |
Cholecystitis and cholelithiasis masking as abdominal crises in sickle cell disease. | ||
Ariyan S, Shessel FS, Pickett LK. Pediatrics. 1976;58(2):252-8. |
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This case led to the investigation of cholelithiasis in sickle cell disease to dispel the following misconceptions. | ||
951141 |
MALE | |
Cholecystitis and cholelithiasis masking as abdominal crises in sickle cell disease. | ||
Ariyan S, Shessel FS, Pickett LK. Pediatrics. 1976;58(2):252-8. |
||
Some physicians and pediatricians believe that (1) cholelithiasis and cholecystitis are uncommon in sickle cell disease; (2) the complications of gallstones are not significant; (3) the operative risk in patients with sickle cell disease is high; (4) these patients with HbSS disease do not live long enough to get into trouble with gallstones. |